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Clinical Research Coordinator - IVRS
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KW
Study group
anthos-Fortrea
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Study
ANT-010
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Environment
Production
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Site
010-9927 - Yuma Clinical Trials, LLC
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Patient
9927001
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EDC
EDC Tasks
9927001
Patient Status
Enrolled
Screening
17 Jun 2025
Day 1
10 Jul 2025
Date of Visit
Inclusion/Exclusion Criteria
Randomization
Vital Signs
Specialty Lab
Hematology
Study Drug SC Administration
Injection Site Reaction
Day 8 (1)
17 Jul 2025
(projected)
Prior and Concomitant Therapies
Procedures and Imagings (1)
Adverse Events and Local Assessments
ePRO Questionnaires (1)
Transfusions (1)
Study Disposition (1)
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9927001
Day 1
Completion Guide
Action
Hematology
Requires Signature
Was the sample collected?
Yes
No
Data Entry Error
Per Query Resolution
New Information
Action
If No, Reason
0 / 200
Data Entry Error
Per Query Resolution
New Information
Action
Date of Sample Collection
...
Jan
Feb
Mar
Apr
May
Jun
Jul
Aug
Sep
Oct
Nov
Dec
DD/MMM/YYYY
Data Entry Error
Per Query Resolution
New Information
Action
Time of Sample Collection
:
24h clock hour:min
Data Entry Error
Per Query Resolution
New Information
Action
Lab Requisition No.
Data Entry Error
Per Query Resolution
New Information
Action
Any Clinically Significant result?
Yes
No
Data Entry Error
Per Query Resolution
New Information
Action
If clinical significant, please ensure it is reported in the 'Additional Medical History' form (screening phase only) or in the 'Adverse Event' form (once randomized to study treatment).
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CRF 419
(Clinical Research Coordinator - IVRS)
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